Accuracy of flow cytometric perforin screening for detecting patients with FHL due to PRF1 mutations

被引：32

作者：

Abdalgani, Manar ^{[1
]}

Filipovich, Alexandra H. ^{[1
]}

Choo, Sharon ^{[2
]}

Zhang, Kejian ^{[3
]}

Gifford, Carrie ^{[1
]}

Villanueva, Joyce ^{[1
]}

Bleesing, Jack J. ^{[1
]}

Marsh, Rebecca A. ^{[1
]}

机构：

[1] Cincinnati Childrens Hosp Med Ctr, Div Bone Marrow Transplantat & Immune Deficiency, Cincinnati, OH 45229 USA

[2] Royal Childrens Hosp, Dept Allergy & Immunol, Melbourne, Vic, Australia

[3] Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

来源：

BLOOD | 2015年 / 126卷 / 15期

关键词：

FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; GENE-MUTATIONS; DEFECTS; JAPAN;

D O I：

10.1182/blood-2015-06-648659

中图分类号：

R5 [内科学];

学科分类号：

100201 [内科学];

摘要：

引用

页码：1858 / 1859

页数：2

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